Alcon AcrySof®

GUDID 00380659909467

AcrySof® IQ Toric IOL Calculator

Alcon Laboratories, Inc.

Intraocular lens web-based calculator software Intraocular lens web-based calculator software Intraocular lens calculation software Intraocular lens calculation software Intraocular lens calculation software Intraocular lens calculation software Intraocular lens calculation software Intraocular lens calculation software Intraocular lens calculation software Intraocular lens calculation software Intraocular lens calculation software Intraocular lens calculation software Intraocular lens calculation software Intraocular lens calculation software Intraocular lens calculation software Intraocular lens calculation software

• Primary Device ID: 00380659909467
• NIH Device Record Key: 0d3a82fc-6ed1-4969-8950-0c87bab08972
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Alcon AcrySof®
• Version Model Number: Version 3
• Company DUNS: 008018525
• Company Name: Alcon Laboratories, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +18008625266
• Email: web.masterus@alcon.com
• Phone: +18008625266
• Email: web.masterus@alcon.com
• Phone: +18008625266
• Email: web.masterus@alcon.com
• Phone: +18008625266
• Email: web.masterus@alcon.com
• Phone: +18008625266
• Email: web.masterus@alcon.com
• Phone: +18008625266
• Email: web.masterus@alcon.com
• Phone: +18008625266
• Email: web.masterus@alcon.com
• Phone: +18008625266
• Email: web.masterus@alcon.com
• Phone: +18008625266
• Email: web.masterus@alcon.com
• Phone: +18008625266
• Email: web.masterus@alcon.com
• Phone: +18008625266
• Email: web.masterus@alcon.com
• Phone: +18008625266
• Email: web.masterus@alcon.com
• Phone: +18008625266
• Email: web.masterus@alcon.com
• Phone: +18008625266
• Email: web.masterus@alcon.com
• Phone: +18008625266
• Email: web.masterus@alcon.com
• Phone: +18008625266
• Email: web.masterus@alcon.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00380659909467 [Primary]

FDA Product Code

• HQL: intraocular lens

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-06-07
• Device Publish Date: 2016-12-13

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• 20380650000556 - LENSX: 2022-11-14 LENSX SOFTFIT PATIENT INTERFACE STEEP,EO